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Hydroxide ion as nucleophile

The rates of the various steps are a function of the pH of the solution, the basicity of the imine, and the reactivity of the aldehyde. Imine protonation enhances reactivity toward either water or hydroxide ion as nucleophiles. Ai-Protonation in the tetrahedral intermediate makes the amine a better leaving group. The zwitterionic intermediate... [Pg.647]

See other pages where Hydroxide ion as nucleophile is mentioned: [Pg.14]    [Pg.123]   
See also in sourсe #XX -- [ Pg.71 , Pg.329 , Pg.330 , Pg.331 , Pg.332 , Pg.333 , Pg.337 , Pg.766 , Pg.852 , Pg.853 , Pg.854 , Pg.855 , Pg.866 ]

See also in sourсe #XX -- [ Pg.329 , Pg.330 , Pg.331 , Pg.332 , Pg.333 , Pg.337 , Pg.716 , Pg.766 , Pg.852 , Pg.853 , Pg.854 , Pg.855 , Pg.866 ]

See also in sourсe #XX -- [ Pg.329 , Pg.330 , Pg.334 , Pg.337 , Pg.338 , Pg.716 , Pg.766 , Pg.852 , Pg.853 , Pg.854 , Pg.855 , Pg.866 ]

See also in sourсe #XX -- [ Pg.306 , Pg.315 , Pg.665 , Pg.712 , Pg.794 , Pg.795 , Pg.796 , Pg.797 , Pg.798 , Pg.808 ]

See also in sourсe #XX -- [ Pg.45 , Pg.326 , Pg.327 , Pg.328 , Pg.333 , Pg.737 , Pg.832 , Pg.833 , Pg.834 , Pg.846 , Pg.903 ]

See also in sourсe #XX -- [ Pg.42 , Pg.309 , Pg.310 , Pg.311 , Pg.316 , Pg.698 , Pg.786 , Pg.787 , Pg.788 , Pg.789 , Pg.799 ]



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Hydroxide ion

Hydroxide ion nucleophile

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